Active Ingredient: GRANISETRON HYDROCHLORIDE
Proprietary Name: KYTRIL
Dosage Form; Route of Administration: SOLUTION; ORAL
Strength: EQ 2MG BASE/10ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N021238
Product Number: 001
Approval Date: Jun 27, 2001
Applicant Holder Full Name: HOFFMANN LA ROCHE INC
Marketing Status:
Discontinued
Patent and Exclusivity Information